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Status |
Public on May 03, 2024 |
Title |
PC_SR_1 |
Sample type |
SRA |
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Source name |
Melanoma biopsy
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Organism |
Homo sapiens |
Characteristics |
treatment: BRAFi+MEKi time: Before the starting of 1 cycle tissue: Melanoma biopsy gender: not collected
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Extracted molecule |
total RNA |
Extraction protocol |
RNA was quantified and mixed at 10ng/µl For RNA-seq analysis, libraries were prepared according to manufacturer's instructions (QuantSeq 3' mRNA-Seq Library Prep Kit FWD for Illumina, Lexogen GmbH) starting from 250ng of total RNA. The amplified fragmented cDNA of 300 bp in size were sequenced in single-end mode using the NovaSeq6000 (Illumina) with a read length of 100 bp
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Data processing |
the reads were trimmed toremove adapter sequences and low-quality ends and reads mapping to contaminating sequences (e.g., ribosomal RNA, phIX control) were filtered-out. Genome_build: Hg38 Supplementary_files_format_and_content: tab-delimited text files include raw counts for each Sample
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Submission date |
Jan 22, 2021 |
Last update date |
May 06, 2024 |
Contact name |
Rossella De Cegli |
E-mail(s) |
decegli@tigem.it
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Phone |
08119230692
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Organization name |
Tigem
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Street address |
Via Campi Flegrei 34
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City |
Pozzuoli |
ZIP/Postal code |
80078 |
Country |
Italy |
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Platform ID |
GPL24676 |
Series (2) |
GSE165337 |
Transcriptomic profile of melanoma clinical samples treated with BRAF and MEK- inhibitors |
GSE165338 |
RNAseq and Small-RNAseq dataset to comprehensively study the miRNA expression profiling of drug-resistant melanoma patients and cell lines |
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Relations |
BioSample |
SAMN17496825 |
SRA |
SRX9920572 |
Supplementary file |
Size |
Download |
File type/resource |
GSM5031711_S273_20200619120606_1_unique_counts.txt.gz |
113.0 Kb |
(ftp)(http) |
TXT |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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